{"count":1,"next":null,"previous":null,"results":[{"gene_data":{"alias":["TCF1ALPHA","TCF10","TCF7L3"],"biotype":"protein_coding","hgnc_id":"HGNC:6551","gene_name":"lymphoid enhancer binding factor 1","omim_gene":["153245"],"alias_name":null,"gene_symbol":"LEF1","hgnc_symbol":"LEF1","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"4:108968701-109090112","ensembl_id":"ENSG00000138795"}},"GRch38":{"90":{"location":"4:108047545-108168956","ensembl_id":"ENSG00000138795"}}},"hgnc_date_symbol_changed":"1991-06-05"},"entity_type":"gene","entity_name":"LEF1","confidence_level":"0","penetrance":null,"mode_of_pathogenicity":"","publications":[],"evidence":["Expert Review Removed","London North GLH","NHS GMS"],"phenotypes":["Sebaceous tumours"],"mode_of_inheritance":"MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","tags":[],"panel":{"id":558,"hash_id":null,"name":"Multiple monogenic benign skin tumours","disease_group":"","disease_sub_group":"","status":"public","version":"0.10","version_created":"2019-06-20T15:15:13.746402Z","relevant_disorders":[],"stats":{"number_of_genes":43,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"Component Of Super Panel","slug":"component-of-super-panel","description":"This panel is a component of a Super Panel"}]}}]}